Human Genome Epidemiology Literature Finder
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Records 1 - 8 (of 8 Records) |
| Query Trace: Disease and AUTS2[original query] |
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| Rare variants in the genetic background modulate cognitive and developmental phenotypes in individuals carrying disease-associated variants. Genetics in medicine : official journal of the American College of Medical Genetics 2018 9 21 (4): 816-825. Pizzo Lucilla, Jensen Matthew, Polyak Andrew, Rosenfeld Jill A, Mannik Katrin, Krishnan Arjun, McCready Elizabeth, Pichon Olivier, Le Caignec Cedric, Van Dijck Anke, Pope Kate, Voorhoeve Els, Yoon Jieun, Stankiewicz Pawe?, Cheung Sau Wai, Pazuchanics Damian, Huber Emily, Kumar Vijay, Kember Rachel L, Mari Francesca, Curró Aurora, Castiglia Lucia, Galesi Ornella, Avola Emanuela, Mattina Teresa, Fichera Marco, Mandarà Luana, Vincent Marie, Nizon Mathilde, Mercier Sandra, Bénéteau Claire, Blesson Sophie, Martin-Coignard Dominique, Mosca-Boidron Anne-Laure, Caberg Jean-Hubert, Bucan Maja, Zeesman Susan, Nowaczyk Ma?gorzata J M, Lefebvre Mathilde, Faivre Laurence, Callier Patrick, Skinner Cindy, Keren Boris, Perrine Charles, Prontera Paolo, Marle Nathalie, Renieri Alessandra, Reymond Alexandre, Kooy R Frank, Isidor Bertrand, Schwartz Charles, Romano Corrado, Sistermans Erik, Amor David J, Andrieux Joris, Girirajan Santho |
| Association of NRG1 and AUTS2 genetic polymorphisms with Hirschsprung disease in a South Chinese population. Journal of cellular and molecular medicine 2018 Jan . Zhang Yan, Xie Xiaoli, Zeng Jixiao, Wu Qiang, Zhang Ruizhong, Zhu Deli, Xia Huim |
| Comprehensive Analysis of Rare Variants of 101 Autism-Linked Genes in a Hungarian Cohort of Autism Spectrum Disorder Patients. Frontiers in genetics 2019 5 10 434. Balicza Péter, Varga Noémi Ágnes, Bolgár Bence, Pentelényi Klára, Bencsik Renáta, Gál Anikó, Gézsi András, Prekop Csilla, Molnár Viktor, Molnár Mária Jud |
Genome-wide association study of germline variants and breast cancer-specific mortality.
British journal of cancer 2019 Mar 120 (6): 647-657. Escala-Garcia Maria, Guo Qi, Dörk Thilo, Canisius Sander, Keeman Renske, Dennis Joe, Beesley Jonathan, Lecarpentier Julie, Bolla Manjeet K, Wang Qin, Abraham Jean, Andrulis Irene L, Anton-Culver Hoda, Arndt Volker, Auer Paul L, Beckmann Matthias W, Behrens Sabine, Benitez Javier, Bermisheva Marina, Bernstein Leslie, Blomqvist Carl, Boeckx Bram, Bojesen Stig E, Bonanni Bernardo, Børresen-Dale Anne-Lise, Brauch Hiltrud, Brenner Hermann, Brentnall Adam, Brinton Louise, Broberg Per, Brock Ian W, Brucker Sara Y, Burwinkel Barbara, Caldas Carlos, Caldés Trinidad, Campa Daniele, Canzian Federico, Carracedo Angel, Carter Brian D, Castelao Jose E, Chang-Claude Jenny, Chanock Stephen J, Chenevix-Trench Georgia, Cheng Ting-Yuan David, Chin Suet-Feung, Clarke Christine L, , Cordina-Duverger Emilie, Couch Fergus J, Cox David G, Cox Angela, Cross Simon S, Czene Kamila, Daly Mary B, Devilee Peter, Dunn Janet A, Dunning Alison M, Durcan Lorraine, Dwek Miriam, Earl Helena M, Ekici Arif B, Eliassen A Heather, Ellberg Carolina, Engel Christoph, Eriksson Mikael, Evans D Gareth, Figueroa Jonine, Flesch-Janys Dieter, Flyger Henrik, Gabrielson Marike, Gago-Dominguez Manuela, Galle Eva, Gapstur Susan M, García-Closas Montserrat, García-Sáenz José A, Gaudet Mia M, George Angela, Georgoulias Vassilios, Giles Graham G, Glendon Gord, Goldgar David E, González-Neira Anna, Alnæs Grethe I Grenaker, Grip Mervi, Guénel Pascal, Haeberle Lothar, Hahnen Eric, Haiman Christopher A, Håkansson Niclas, Hall Per, Hamann Ute, Hankinson Susan, Harkness Elaine F, Harrington Patricia A, Hart Steven N, Hartikainen Jaana M, Hein Alexander, Hillemanns Peter, Hiller Louise, Holleczek Bernd, Hollestelle Antoinette, Hooning Maartje J, Hoover Robert N, Hopper John L, Howell Anthony, Huang Guanmengqian, Humphreys Keith, Hunter David J, Janni Wolfgang, John Esther M, Jones Michael E, Jukkola-Vuorinen Arja, Jung Audrey, Kaaks Rudolf, Kabisch Maria, Kaczmarek Katarzyna, Kerin Michael J, Khan Sofia, Khusnutdinova Elza, Kiiski Johanna I, Kitahara Cari M, Knight Julia A, Ko Yon-Dschun, Koppert Linetta B, Kosma Veli-Matti, Kraft Peter, Kristensen Vessela N, Krüger Ute, Kühl Tabea, Lambrechts Diether, Le Marchand Loic, Lee Eunjung, Lejbkowicz Flavio, Li Lian, Lindblom Annika, Lindström Sara, Linet Martha, Lissowska Jolanta, Lo Wing-Yee, Loibl Sibylle, Lubinski Jan, Lux Michael P, MacInnis Robert J, Maierthaler Melanie, Maishman Tom, Makalic Enes, Mannermaa Arto, Manoochehri Mehdi, Manoukian Siranoush, Margolin Sara, Martinez Maria Elena, Mavroudis Dimitrios, McLean Catriona, Meindl Alfons, Middha Pooja, Miller Nicola, Milne Roger L, Moreno Fernando, Mulligan Anna Marie, Mulot Claire, Nassir Rami, Neuhausen Susan L, Newman William T, Nielsen Sune F, Nordestgaard Børge G, Norman Aaron, Olsson Håkan, Orr Nick, Pankratz V Shane, Park-Simon Tjoung-Won, Perez Jose I A, Pérez-Barrios Clara, Peterlongo Paolo, Petridis Christos, Pinchev Mila, Prajzendanc Karoliona, Prentice Ross, Presneau Nadege, Prokofieva Darya, Pylkäs Katri, Rack Brigitte, Radice Paolo, Ramachandran Dhanya, Rennert Gadi, Rennert Hedy S, Rhenius Valerie, Romero Atocha, Roylance Rebecca, Saloustros Emmanouil, Sawyer Elinor J, Schmidt Daniel F, Schmutzler Rita K, Schneeweiss Andreas, Schoemaker Minouk J, Schumacher Fredrick, Schwentner Lukas, Scott Rodney J, Scott Christopher, Seynaeve Caroline, Shah Mitul, Simard Jacques, Smeets Ann, Sohn Christof, Southey Melissa C, Swerdlow Anthony J, Talhouk Aline, Tamimi Rulla M, Tapper William J, Teixeira Manuel R, Tengström Maria, Terry Mary Beth, Thöne Kathrin, Tollenaar Rob A E M, Tomlinson Ian, Torres Diana, Truong Thérèse, Turman Constance, Turnbull Clare, Ulmer Hans-Ulrich, Untch Michael, Vachon Celine, van Asperen Christi J, van den Ouweland Ans M W, van Veen Elke M, Wendt Camilla, Whittemore Alice S, Willett Walter, Winqvist Robert, Wolk Alicja, Yang Xiaohong R, Zhang Yan, Easton Douglas F, Fasching Peter A, Nevanlinna Heli, Eccles Diana M, Pharoah Paul D P, Schmidt Marjanka |
| Effect of AUTS2 gene rs6943555 variant in male patients with schizophrenia in a Turkish population. Gene 2020 6 756 144913. Ozsoy Filiz, Karakus Nevin Balci, Yigit Serbulent, Kulu Muber |
| Evaluation of candidate genes in a Chinese cohort of atypical Rolandic epilepsy. Epileptic disorders : international epilepsy journal with videotape 2021 Jul . Hu Xiaoyue, Tang Jihong, Hua Ying, Wang Yanping, Huang Ji |
| Trans-ancestry, Bayesian Meta-analysis Discovers 20 Novel Risk Loci for Inflammatory Bowel Disease in an African American, East Asian, and European Cohort. Human molecular genetics 2022 10 . Cordero Roberto Y, Cordero Jennifer B, Stiemke Andrew B, Datta Lisa W, Buyske Steven, Kugathasan Subra, McGovern Dermot P B, Brant Steven R, Simpson Claire |
| Genome-wide association analysis reveals the associations of NPHP4, TYW1-AUTS2 and SEMA6D for Behçet's disease and HLA-B*46:01 for its intestinal involvement. Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver 2023 11 . Eun Suk Jung, David Ellinghaus, Frauke Degenhardt, Akira Meguro, Seik-Soon Khor, Sören Mucha, Mareike Wendorff, Simonas Juzenas, Nobuhisa Mizuki, Katsushi Tokunaga, Seung Won Kim, Min Goo Lee, Stefan Schreiber, Won Ho Kim, Andre Franke, Jae Hee Che |
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